Global PDM & Quality Process Expert

Johnson & Johnson Innovative Medicine; Beerse; Sur place; EUR 60 000 - 96 000; Plein temps

Avantages offerts par ce poste

Annual bonus

Well-being programs

Résumé du poste

Johnson & Johnson Innovative Medicine is seeking a Specialist, Process & Data Management to join the QM&D organization. You will translate regulatory and business needs into integrated processes, training materials, and qualification solutions across global R&D teams.

In this role, you’ll collaborate with Therapeutic Areas, Clinical Development, Medical Safety, Regulatory Affairs, and R&D Quality to drive compliant process improvement and data-centric content.

Qualifications

• Knowledge of global pre-clinical and clinical compliance regulations.
• Awareness of regulatory and legal requirements within life sciences.
• Experience contributing to process improvement and qualification activities.
• Ability to work effectively in a matrix and virtual environment.

Responsabilités

• Lead ARR and Quality Framework Integration initiatives.
• Develop and implement compliant end-to-end processes.
• Create and maintain training and qualification materials within the GxP QM framework.
• Perform requirement assessment and integration across the QMS.
• Coordinate content management and qualification transformation initiatives.

Connaissances

Analytical reasoning

Business behavior

Business savvy

Compliance management

Continuous improvement

CQI

Data reporting

Goal attainment

Problem solving

Process optimization

Project management

Quality assurance

Quality control

Quality standards

Training administration

Training delivery methods

Training needs analysis

Training people

Formation

Bachelor’s degree in Science, Business, or related field

Outils

Project management tools

Process mapping tools

AI concepts and frameworks awareness

Description du poste

Johnson & Johnson Innovative Medicine is seeking a Specialist, Process & Data Management to join the QM&D organization. You will translate regulatory and business needs into integrated processes, training materials, and qualification solutions across global R&D teams.

In this role, you’ll collaborate with Therapeutic Areas, Clinical Development, Medical Safety, Regulatory Affairs, and R&D Quality to drive compliant process improvement and data-centric content.